Cis tert-Butyl 4-aminocyclohexylcarbamate → trans-(4-{[4-(2-Cyclopropylmethoxy-5-fluoro-4-methoxy-phenyl)-5H-pyrrolo[3,2-d]pyrimidine-7-carbonyl]-amino}-cyclohexyl)-carbamic acid tert-butyl ester
Reaktionsgleichung
[C:27]([CH3:28])([CH3:29])([CH3:30])[O:31][C:32]([NH:33][CH:34]1[CH2:35][CH2:36][CH:37]([NH2:40])[CH2:38][CH2:39]1)=[O:41].[CH:1]1([CH2:4][O:5][c:6]2[c:7](-[c:15]3[c:16]4[c:17]([n:18][cH:19][n:20]3)[c:21]([C:24](=[O:25])[OH:26])[cH:22][nH:23]4)[cH:8][c:9]([F:14])[c:10]([O:12][CH3:13])[cH:11]2)[CH2:2][CH2:3]1>>[CH:1]1([CH2:4][O:5][c:6]2[c:7](-[c:15]3[c:16]4[c:17]([n:18][cH:19][n:20]3)[c:21]([C:24](=[O:25])[NH:40][CH:37]3[CH2:36][CH2:35][CH:34]([NH:33][C:32]([O:31][C:27]([CH3:28])([CH3:29])[CH3:30])=[O:41])[CH2:39][CH2:38]3)[cH:22][nH:23]4)[cH:8][c:9]([F:14])[c:10]([O:12][CH3:13])[cH:11]2)[CH2:2][CH2:3]1Komponenten
3
Edukt 2
Produkt 1
Quellen und Nachweise
- ORD-Eintrag
- ord-b3218187f0d9422a8a1c55a115e4293a
- Quelldatensatz
- Training data from https://doi.org/10.1039/C8SC04228D (2/10)